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(3-nitrophenyl) N-[4-(4-chlorophenyl)sulfonylphenyl]carbamate

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Identification
Molecular formula
C19H13ClN2O6S
CAS number
848689-64-1
IUPAC name
(3-nitrophenyl) N-[4-(4-chlorophenyl)sulfonylphenyl]carbamate
State
State

At room temperature, the compound is typically in a solid state, appearing as a crystalline powder. The stability at ambient conditions is relatively good if stored properly, away from moisture and direct sunlight exposure.

Melting point (Celsius)
159.00
Melting point (Kelvin)
432.15
Boiling point (Celsius)
554.00
Boiling point (Kelvin)
827.15
General information
Molecular weight
407.83g/mol
Molar mass
407.8140g/mol
Density
1.4280g/cm3
Appearence

The compound typically appears as an off-white to pale yellow crystalline powder. It is important to ensure the packaging is well sealed due to its hygroscopic nature, which means it can absorb moisture from the air.

Comment on solubility

Solubility of (3-nitrophenyl) N-[4-(4-chlorophenyl)sulfonylphenyl]carbamate

The solubility of (3-nitrophenyl) N-[4-(4-chlorophenyl)sulfonylphenyl]carbamate can be influenced by various factors, making it a complex subject to discuss. Here are some key points regarding its solubility properties:

  • Polar vs. Non-Polar Characteristics: This compound contains both polar and non-polar functional groups, which could lead to moderate solubility in polar solvents like methanol or ethanol.
  • Hydrogen Bonding: The presence of a carbamate group suggests potential for hydrogen bonding with water, which may enhance solubility.
  • pH Dependence: The solubility might vary significantly with pH, as the ionizable groups can interact differently under acidic or basic conditions.
  • Temperature Effects: As with many solid compounds, an increase in temperature typically increases solubility; thus, heating may facilitate dissolution.

In summary, while the solubility of (3-nitrophenyl) N-[4-(4-chlorophenyl)sulfonylphenyl]carbamate is likely to be moderate to good in certain solvents, careful consideration of factors such as solvent polarity, pH, and temperature is crucial for predicting its behavior in various environments.

Interesting facts

Interesting Facts about (3-nitrophenyl) N-[4-(4-chlorophenyl)sulfonylphenyl]carbamate

(3-nitrophenyl) N-[4-(4-chlorophenyl)sulfonylphenyl]carbamate is a fascinating compound that demonstrates the complexity and diversity of organic chemistry. This compound is particularly noteworthy due to its unique structural features, which contribute to its potential applications in various fields, including pharmaceuticals and agrochemicals.

Key Features

  • Biological Activity: The presence of both nitro and sulfonyl groups in its structure hints at potential biological activities such as antimicrobial or anti-inflammatory properties, making it a subject of interest in drug development.
  • Structural Diversity: Incorporation of a carbamate group indicates its potential use in creating derivatives that may enhance its activity or modify its interaction with biological targets.
  • Chlorine Substitution: The chlorophenyl moiety can influence the compound's electronic characteristics, possibly improving its stability or solubility in different environments.

In various chemical research contexts, this compound serves as a model for understanding essential chemical interactions. For instance, it can be particularly instructive when studying:

  1. Reactivity Patterns: The reactivity of various functional groups within the molecule showcases how subtle changes in structure can significantly alter chemical behavior.
  2. Structure-Activity Relationships: Investigating how modifications to the nitrophenyl and sulfonyl groups affect biological activity can provide insights into design strategies for new therapeutic agents.

As emphasized by chemists, the synthesis of such compounds can lead to exciting discoveries. The complexity of (3-nitrophenyl) N-[4-(4-chlorophenyl)sulfonylphenyl]carbamate reminds us that every small molecular modification can pave the way for breakthroughs in both basic research and real-world applications. Exploring this compound further may reveal even greater secrets about its potential uses in science and industry.

Synonyms
BRN 3018102
CARBANILIC ACID, p-((p-CHLOROPHENYL)SULFONYL)-, m-NITROPHENYL ESTER
14193-07-8
p-((p-Chlorophenyl)sulfonyl)carbanilic acid m-nitrophenyl ester
DTXSID40161861
N-(4-(4'-Chlorophenylsulfonyl)phenyl)-m-nitrophenyl-urethane [French]
N-(4-(4'-Chlorophenylsulfonyl)phenyl)-m-nitrophenyl-urethane
DTXCID5084352